rs267607106

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs267607106(C;G)

Make rs267607106(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

35249968

Gene

TBX20

is a	snp
is	mentioned by
dbSNP	rs267607106
dbSNP (classic)	rs267607106
ClinGen	rs267607106
ebi	rs267607106
HLI	rs267607106
Exac	rs267607106
Gnomad	rs267607106
Varsome	rs267607106
LitVar	rs267607106
Map	rs267607106
PheGenI	rs267607106
Biobank	rs267607106
1000 genomes	rs267607106
hgdp	rs267607106
ensembl	rs267607106
geneview	rs267607106
scholar	rs267607106
google	rs267607106
pharmgkb	rs267607106
gwascentral	rs267607106
openSNP	rs267607106
23andMe	rs267607106
SNPshot	rs267607106
SNPdbe	rs267607106
MSV3d	rs267607106
GWAS Ctlg	rs267607106

Max Magnitude

0

ClinVar
Risk	rs267607106(G;G)
Alt	rs267607106(G;G)
Reference	Rs267607106(C;C)
Significance	Pathogenic
Disease	Atrial septal defect 4
Variation	info
Gene	TBX20
CLNDBN	Atrial septal defect 4
Reversed	1
HGVS	NC_000007.13:g.35289580G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004897.2,